Canonical Allele Identifier: CA721246590
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs1469821456
gnomAD v3: 16-4951388-C-T
gnomAD v4: 16-4951388-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951388C>T , CM000678.2:g.4951388C>T GRCh38
NC_000016.9:g.5001389C>T , CM000678.1:g.5001389C>T GRCh37
NC_000016.8:g.4941390C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000592772.1:c.-92+9176G>A ENSP00000467699.1:n.-92+9176G>A